Robbins Ch. 20 - The Kidney II Flashcards
MPGN
pattern, not disease
-proliferation of mesangium and capillaries
can be combined - nephrotic/nephritic
proliferating mesangium splits BM
subendothelial deposits, IgG, C3, C1q, granular
MPGN type I
prognosis of MPGN type 1
50% to ESRD within 10 years
alpha-1 antitrypsin deficiency
familial emphysema
-MPGN Type 1 - secondary form
cryoglobulinemia
Hep B/C - MPGN type 1 - secondary form
excessive alternate complement pathway
MPGN, type II, dense deposit disease
C3NeF
dense deposit disease
prognosis of DDD
50% to ESRD
90% recurrence in transplants
berger disease
IgA nephropathy
most common GN worldwide
mesangial IgA deposits
IgA nephropathy
celiac disease
IgA nephropathy
clinical for IgA nephropathy
20-30yo, males
gross hematuria following infection of resp, GU, urinary tract
EPISODIC hematuria
prognosis for IgA nephropathy
15-40% to ESRD over 20 years
recurrence frequent in transplants
episodic hematuria
IgA nephropathy
berger disease
not systemic disease - IgA nephropathy
henoch schonlein purpura
is systemic disease - IgA nephropathy
- skin lesions on buttocks
- systemic vasculitis
nerve deafness, eye disorders, hematuria
alport syndrome
alport genetics
85% X-linked - males full / females only hematuria**
also autosomal dominant and recessive forms
basket weave GBM
alport syndrome
age for alport
5-20 years old
renal failure age 20-50 years old
benign familial hematuria
thin basement membrane lesion
excellent prognosis
mutations in alpha3, 4 of collagen 4
thin basement membrane lesion